Canonical Allele Identifier: PA2826630220
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 483857
ClinVar RCV Id: RCV000575116 RCV002298682
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Lys174Arg
CA346745443
NM_001281493.2:c.521A>G